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Usage

Uses

Used in Materials Science:
(1,1'-phenyl-1,1'-silacyclohex-1-yl)disiloxane is utilized as a component in materials science for its distinctive silicon-containing structure, which can contribute to the development of novel materials with specific properties.
Used in Organic Synthesis:
In organic synthesis, (1,1'-phenyl-1,1'-silacyclohex-1-yl)disiloxane serves as a valuable intermediate or precursor. Its unique structure allows it to be employed in the synthesis of other silicon-containing compounds, expanding the range of possible organic reactions and products.
Used in Silicon-Based Polymers Development:
(1,1'-phenyl-1,1'-silacyclohex-1-yl)disiloxane is used as a monomer or building block in the development of silicon-based polymers. Its incorporation into polymer structures can lead to materials with enhanced properties, such as thermal stability or specific chemical reactivity.
Used as a Precursor in Silicon-Containing Compounds Synthesis:
(1,1'-phenyl-1,1'-silacyclohex-1-yl)disiloxane is used as a precursor in the synthesis of other silicon-containing compounds. Its unique structure makes it a promising candidate for creating new compounds with potential applications in various industries.
Further research is likely needed to fully understand and exploit the potential applications of (1,1'-phenyl-1,1'-silacyclohex-1-yl)disiloxane, as its unique silicon-containing structure may offer additional benefits in a range of applications.

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Relevant academic research and scientific papers

Conformational Analysis of (1,1′-Phenyl-1,1′-silacyclohex-1-yl)disiloxane. DFT and Low-Temperature 13C NMR Spectroscopy Study

The DFT and MP2 theoretical conformational analysis of the recently synthesized (1,1′-phenyl-1,1′-silacyclohex-1-yl)disiloxane has revealed the energetic preference of the Phax,Phax conformer. The Phax,Phax: Ph

1-Phenyl-1-halo-1-silacyclohexanes

The approaches to synthesis of 1-phenyl-1-halo-1-silacyclohexanes C5H10Si(Ph)X (X = F, Cl, Br) have been examined. 1-Phenyl-1-chloro-1-silacyclohexane has been prepared via the known reaction of phenyltrichlorosilane with dimagnesium

1-Phenyl-1-X-1-silacyclohexanes (X = MeO, OH, Me2N)

By the reaction of nucleophilic substitution of chlorine in 1-phenyl-1-chloro-1-silacyclohexane new 1-phenyl-1-X-1-silacyclohexanes (Х = , ОН, Ме2N) have been synthesized and their stability with respect to the formation of (1,1′-phenyl-1,1′-silacyclohex-1-yl)disiloxane have been investigated.

1-t-Butyl-1-phenyl-1-silacyclohexane: Synthesis, conformational analysis in gas and solution by GED, FT-IR and theoretical calculations

1-t-Butyl-1-phenyl-1-silacyclohexane 1, the first disubstituted silacyclohexane with the most bulky substituent, t-Bu group, at silicon, was synthesized via the sequence of reactions PhSiCl3 → Ph(Cl)Si(CH2)5 → Ph(t-Bu)Si(C